Canonical Allele Identifier: CA2174009929
Gene: SLC28A2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1754980456

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45251682G>A , CM000677.2:g.45251682G>A GRCh38
NC_000015.9:g.45543880G>A , CM000677.1:g.45543880G>A GRCh37
NC_000015.8:g.43331172G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120335.1:n.571C>T